UHC4RareDiseases

RDI and EURORDIS have partnered to develop the UHC4RareDiseases campaign. The campaign aims to enable patient organisations and the public to call for Universal Health Coverage (UHC) policies and programmes that include rare diseases.

The UHC4RareDiseases toolkit offers practical tools that you can use to raise awareness and ask policymakers to address rare diseases in order to fulfil their commitment to UHC and Health for All.

UHC ensures all people, everywhere, can access quality health services with financial protection.

All UN Member States have agreed to try to achieve Universal Health Coverage by 2030, as part of the Sustainable Development Goals. In 2019, member countries adopted the UN Political Declaration on UHC. The Declaration includes rare diseases! It commits all governments to strengthen efforts to address rare diseases in their plans to achieve UHC.

UHC4RareDiseases comes in the lead up to UHC Day (December 12th) and the Rare Disease Day campaign which calls for equity for patients and families living with a rare disease.

By using the UHC4RareDiseases advocacy and communication tools, rare disease communities around the world can urge their governments to include rare diseases in their countries’ UHC strategies and essential health service packages.

How to use the toolkit

Watch the #UHC4RareDiseases Tutorial

Presented by EURORDIS CEO Yann Le Cam and RDI Director Flaminia Macchia

Download the Toolkit

  1. FACT SHEET on UHC and rare diseases
  2. LETTER TEMPLATE to send to policymakers/ MPs/ local or national Health Ministries
  3. BRIEFING PACKAGE
  4. SOCIAL MEDIA KIT

For more information and editable versions of the template letter and factsheet, contact Clara Hervas, EURORDIS/RDI Public Affairs Manager, clara.hervas@eurordis.org

Find more GIFs in the social media kit

Page created: 23/09/2020
Page last updated: 07/10/2020
 
 
Die Stimme der Menschen mit seltenen Krankheiten in EuropaEURORDIS Die internationale Stimme für Menschen mit seltenen KrankheitenRare Disease International Ein moderiertes mehrsprachiges Forum, das Patienten, Familien und Experten zum Erfahrungsaustausch zusammenführt. RareConnect Das Rare Barometer Programm ist eine EURORDIS-Initiative, die Umfragen durchführt und die Erfahrungen von Patienten mit seltenen Erkrankungen in Fakten und Zahlen umwandelt, die wiederum Entscheidungsträgern vermittelt werden können.Rare Barometer Eine internationale Aufklärungskampagne, die jedes Jahr am letzten Tag im Februar stattfindet. Der Tag der Seltenen Erkrankungen ist eine EURORDIS-InitiativeRare Disease Day Nehmen Sie am größten Zusammentreffen von Interessenvertretern für seltene Krankheiten in Europa teil und besuchen Sie die zweijährliche Europäische Konferenz für Seltene Krankheiten und Orphan-Produkte (ECRD). ECRD ist eine EURORDIS-InitiativeEuropean Conference on Rare Diseases